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Age group differences in association between IADL decline and depressive symptoms in community-dwelling elderly
BMC Geriatrics volume 19, Article number: 309 (2019)
Abstract
Background
Instrumental Activities of Daily Living (IADL) is an indicator of whether a community-dwelling elderly can live independently. IADL decline was reported to be associated with aging and depression. The present study aimed to investigate whether the association between IADL decline and depressive symptoms differs with aging, using two age groups of community-dwelling Japanese elderly in their 70s and 80s.
Methods
We conducted longitudinal analysis among participants in their 70s and 80s at the baseline from Septuagenarians, Octogenarians, Nonagenarians Investigation with Centenarians (SONIC) study. IADL was assessed by The Tokyo Metropolitan Institute of Gerontology (TMIG) index of competence. As a main predictor, depressive symptoms were measured by the five-item version of the Geriatrics Depression Scale (GDS-5). As possible confounders, we considered cognitive function, body mass index, solitary living, education, economic status, medical history of stroke and heart disease, hypertension, dyslipidemia, diabetes, and sex. We obtained odds ratios (ORs) of IADL decline for having depressive symptoms in each age group (70s/80s) and tested interactions between depressive symptoms and age groups in relation to IADL decline in 3 years by logistic regression. Additionally, to confirm age group differences, we conducted multiple group analysis.
Results
There were 559 participants in their 70s and 519 in their 80s. Compared to participants without depressive symptoms, those with depressive symptoms had higher OR of IADL decline in 70s (OR [95% CI] = 2.33 [1.13, 4.78]), but not in 80s (OR [95% CI] = 0.85 [0.46, 1.53]). There were significant interactions between depressive symptoms and age groups in relation to IADL decline (p-value = 0.03). Multiple group analyses showed differences between the age groups by Akaike information criterion (AIC), and ORs (95%CI) decline for depressive symptoms was 2.33 (1.14, 4.77) in 70s and 0.85 (0.47, 1.54) in 80s.
Conclusion
The association of depressive symptoms and IADL decline during the 3 years was significantly different between the 70s and 80s age groups, and significant association was found only in people in their 70s. Detecting depressive symptoms may be a key for preventing IADL decline in people in their 70s and not for those in their 80s.
Background
Among the population aged 65 years and older, 35% of people suffer from disability (e.g., activities of daily living (ADL) decline and instrumental ADL (IADL) decline) [1], which can make it difficult for people to live independently. IADL represents abilities for using public transportation, shopping for daily necessities, preparing meals, paying bills, managing a bank account, and so on [2], meaning that IADL is a key factor for the elderly to live independently, socially, and healthily.
Depressive symptom is an important risk factor for IADL decline [3, 4]. A previous epidemiological study has reported that depressive symptoms increased the risk of difficulties in ADL and IADL [3] among community-dwelling Japanese elderly people aged 75 years and older (n = 581). Another previous study using a prospective cohort design has shown that depressive symptoms predicted IADL decline in 3–4 years [4] among people aged 65 years and older in the United States of America (n = 3052).
However, the association between depressive symptoms and IADL decline may be different across the age groups of those in their 70s and 80s because of the possible following reasons. The prevalence of impaired IADL in people aged 80 years and over was almost twice than that of people aged 70 to 79 years [5]. Additionally, the prevalence of depression in people aged 85 years and over was twice than that in people aged 70 to 74 years [6]. Finally, a previous cross-sectional research of which participants were community-dwelling adults aged 57 to 99 years in Netherlands (n = 5279) reported that depression was significantly associated with IADL decline in people aged 65 to 74 years old (P = 0.01), but not significantly in people aged 75 years and over (P = 0.07) [7]. However, few studies have investigated whether the association of depressive symptoms with IADL decline was different between age groups.
The present study aimed to investigate whether the association between IADL decline and depressive symptoms was different between the age groups, 70s and 80s, in community-dwelling Japanese elderly.
Methods
Participants
This paper used a longitudinal design (3-year follow-up period) from the Septuagenarians, Octogenarians, Nonagenarians Investigation with Centenarians (SONIC) study, an ongoing study since 2010. Participants were selected from urban and rural areas in Western and Eastern Japan: Itami City (urban) and Asago City (rural) in Hyogo prefecture (Western Japan); Itabashi Ward (urban) and Nishitama District (rural) in Tokyo prefecture (Eastern Japan). We sent invitation letters of participation in the SONIC study to residents between 2010 and 2013, of which 1000 participants were aged 69–71, 973 aged 79–81, and 272 aged 89–91 years, with follow-ups of 3-year intervals. This study was approved by the Institutional Review Board of Osaka University Graduate School of Medicine, Dentistry and Human Sciences (Osaka, Japan) and the Tokyo Metropolitan Geriatric Hospital and Institute of Gerontology (Tokyo, Japan). All participants provided written informed consent to participate.
The eligibility criteria for the present paper were the participants of the SONIC study 1) who were 69–71 years old in 2010 as the baseline for the 70s age group, and who were aged 79–81 years old in 2011 as the baseline for the 80s age group, 2) whose IADL were not declining and were a full score at the baseline, and 3) who participated in the SONIC study at the baseline and periods of the 3-year follow-ups. Participants with missing information on IADL and depressive symptoms were excluded (122 for 70s, and 51 for 80s). The number of participants of the present paper was 1078, consisting of 539 in the 70s group and 519 in the 80s group.
The IADL assessment
In the present study, IADL was assessed by an IADL subscale, consisting of five questions from The Tokyo Metropolitan Institute of Gerontology (TMIG) index of competence [2]. Participants answered each question with “yes” or “no” indicating whether or not the individual is able to do a particular activity (i.e. using public transportation, shopping, food preparation, paying bills, handling bank account). The number of items answered “yes” indicated the total score of the IADL subscale, ranging from 0 (worst) to 5 (best). We considered participants whose IADL scores were 0–4 as participants with IADL decline [8]. We assessed the IADL at baseline and at periods of the 3-year follow-ups.
Depression symptoms
To assess depressive symptoms, we used the five-item version of the Geriatric Depression Scale (GDS-5) [9]. Participants answered each question with “yes” or “no”, providing a total GDS score of 0–5; a higher score indicated a more severe depressive state. Participants with a total GDS-5 score < 2 were defined to have non-depressive symptoms, and those with a total GDS-5 score≧2 were defined to have depressive symptoms [10]. The cut-off point for depressive symptoms has been reported to have a sensitivity of 0.97 and specificity of 0.85 for depressive symptoms assessed by Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition (DSM-IV) criteria [9]. We also used the cut-off point of the GDS-5, and categorized the present participants as having either non-depressive or depressive symptoms.
Possible confounders
As possible confounders, the following variables were considered: sex, cognitive function, economic condition, education, solitary living, histories of stroke and heart disease, hypertension, dyslipidemia, diabetes, and body mass index (BMI), which were based on previous studies of the associations between depressive symptoms [11, 12] and IADL decline.
In the present study, cognitive function was assessed by the Japanese version of the Montreal Cognitive Assessment (MoCA-J) [13]. The MoCA-J test is a validated tool used to assess global cognition and was developed to assist in the diagnosis of MCI [14]. Participants take approximately 10 min to take the MoCA-J test. The MoCA-J assesses seven cognitive functions: visuospatial ability (3 points), naming task (3 points), attention task (6 points), language (3 points), abstraction task (2 points), delayed recall (5 points), and orientation (6 points). Ranging from a total of 0 to 30 points, a lower score indicated a more sever impairment of cognitive function.
Height was measured using calibrated height meters to the nearest 0.1 cm while the participant stood erect without shoes. This measurement was then converted to meters. Weight was measured using calibrated body weight machine to the nearest 0.1 kg in light clothing without shoes. BMI was calculated as the weight in kilograms divided by the square of the height in meters (kg/m2). Hypertension was defined by medication use for hypertension or BP level (i.e., systolic BP > 150 mmHg or diastolic BP > 90 mmHg). To measure the BP levels, physicians and trained nurses used the mercury sphygmomanometer. BP was measured twice on each arm in a sitting position. The average of the first and second measurements on each arm was used for analysis. The present study defined dyslipidemia by medication use of dyslipidemia, low-density lipoprotein cholesterol≧140 mg/dL, high-density lipoprotein cholesterol< 40 mg/dL, or triglyceride≧150 mg/dL. In the present study, diabetes was defined by medication use of diabetes, hemoglobin A1c≧7.0%, or casual plasma glucose concentration≧200 mg/dL. Those definitions were based on the criterion of Japanese guidelines for aged people [15,16,17]. Histories of stroke and heart disease were collected by a self-reported questionnaire answered by “yes” or “no” in health check-ups.
We categorized education years into two categories (< 16 years / ≥ 16 years) corresponding to graduation from University or not. Economic condition was based on subjective satisfaction of household income by three options (Dissatisfying, Neutral, Satisfying) in the questionnaire, which we further categorized into two for analysis (Dissatisfying / Neutral or Satisfying). We gained information about solitary living from the question, “who do you live with?” This was answered by one of five options (No one, Spouse, Parents(−in-law), Children(−in-law), Others). We grouped these answers into two categories for analysis to indicate solitary living by the option “No one” and non-solitary living by all the other options.
Statistical analyses
To investigate the association between depressive symptoms and IADL decline in 3 years, we conducted logistic regression models stratified by the age groups (70s / 80s) to obtain odds ratios (ORs) and 95% confidence intervals (CI). For this we used two models. In the first model (Model 1), the association of depressive symptoms with IADL decline was adjusted for sex (male / female) and cognitive function assessed by the MoCA-J. In the second model (Model 2), the association was adjusted for sex, cognitive function, BMI, histories of stroke (yes/no) and heart disease (yes/no), solitary living (yes/no), economic condition (Dissatisfying / Neutral or Satisfying), education (≦16 years / > 16 years), hypertension (yes/no), dyslipidemia (yes/no), and diabetes (yes/no).
To investigate whether the association of the baseline depressive symptoms with IADL decline in 3 years was different between the two age groups of 70s and 80s, we investigated interactions between depressive symptoms and age groups in relation to IADL decline in 3 years by logistic regression analyses and also conducted multiple group analysis. Multiple group analysis is an analysis of a framework of structural equation modeling method. This analysis can estimate simultaneously across groups [18, 19]. We compared an equality constrained model with an unconstrained model to investigate whether the association of depressive symptoms with IADL decline was different between the age groups (i.e., 70’s and 80’s). In an equality constrained model, regression coefficients of depressive symptoms are estimated to be equal between the age groups. On the other hand, in an unconstrained model, regression coefficients of depressive symptoms are freely estimated across the age groups. We compared those two models by Akaike information criterion (AIC), a good-of-fit index with considering the rule of parsimony. When the unconstrained model is better than the equality constrained model, we can interpret that the regression coefficients of depressive symptoms are not equal across the age groups, meaning that the associations between depressive symptoms and IADL decline are significantly different between the age groups. On the other hand, when the equality constrained model is better, we can interpret that the regression coefficients of depressive symptoms are equal across the groups, meaning that the associations are not significantly different between the groups. In the present study, we set estimates of regression coefficients of depressive symptoms on the IADL decline equal between 70s age groups and 80s age groups in the equality constrained model. We obtained odds ratios (ORs) and 95% confidence intervals (CI).
Logistic regression analysis was performed by statistical software R version 3.4.0. In addition, Multiple group analysis was conducted by Mplus version8.3 [20].
Results
Of the eligible 1078 participants, 156 (28.9%) and 199 (38.3%) participants suffered from depressive symptoms in the 70s and 80s groups, respectively. The baseline characteristics of the present participants were summarized in Table 1. In the 70s group, of the 156 participants with depressive symptoms, 21 (13.5%) had IADL decline in 3 years, and of the 383 participants without that, 25 (6.5%) had IADL decline. In the 80s group, of the 199 participants with depressive symptoms, 22 (11.1%) had IADL decline in 3 years, and of the 320 participants without that, 42 (13.1%) had IADL decline. (Fig. 1).
We investigated the association of depressive symptoms with IADL decline in 3 years for the 70s age group and the 80s age group (Table 2). IADL decline was significantly associated with depressive symptoms in the 70s age group, but not in 80s. When sex and cognitive function were adjusted, ORs (95%CI) of IADL decline for having depressive symptoms compared with not having depressive symptoms were 2.11 (1.10, 4.03) in 70s and 0.81 (0.46, 1.40) in 80s. We obtained similar results in model 2 as a fully-adjusted model. Additionally, we found significant interactions between depressive symptoms and age groups in relation to IADL decline: those p-values were 0.02 in Model1 and 0.03 in Model2 (Table 2).
To focus on the age group differences (70s/80s) for the association, we conducted multiple group analysis (Table 3). Compared with the unconstrained models, the equality models were worse based on AICs (2128 for equity vs 2125 for unconstrained in Model 1 and 1961 vs 1964 in Model 2). For unconstrained model in Model 1, ORs of IADL decline for depressive symptoms compared with no having depressive symptoms were 2.11 (1.11, 4.03) in 70s and 0.81 (0.47, 1.41) in 80s. We obtained similar results in model 2 as a fully-adjusted model (ORs = 2.33 95%CI, 1.14, 4.77 in 70s; ORs = 0.85 95%CI, 0.47, 1.54 in 80s).
Discussion
The present study aimed to investigate whether the association of depressive symptoms with IADL decline was different in elderly people in their 70s and in their 80s. Logistic regression analysis showed that depressive symptoms were significantly associated with IADL decline in 70s (OR = 2.33, 95%CI, 1.13, 4.78), but not in 80s (OR = 0.85, 95%CI, 0.46, 1.53). Additionally, we found significant interaction between depressive symptoms and the age groups in relation to the IADL decline (p = 0.03). Furthermore, the multiple group analyses showed that, the unconstrained model was better than the equality constrained model for the association based on AIC, meaning there was different between 70s and 80s on the association of depressive symptoms with the IADL decline.
The present result of the significant association of depressive symptoms with IADL decline in the 70s group by logistic regression and multiple group analysis were similar to the previous study [21]. The present results might be due to the following possible reasons. According to a previous study [21], depressive symptoms such as fatigue, sleep disturbance, and loss of appetite could reduce motivation for treatments and preventions of disabilities. Additionally, people with depressive symptoms were also undermined their resistance to disabilities including IADL decline [21].
The present study showed significant association of depressive symptoms with IADL decline in the 70s group but not in the 80s. Possible reasons for this could be as follows. First, in a previous study [22], depression was found to be common among people aged 85 years and over; its prevalence was 15.3% [6]. The participants’ age in this previous study was similar to that in the present study. Second, the proportion of solitary living was high only in the 80s age group with depressive symptoms in the present study (Additional file 1: Table S1). People living alone in communities may not need significant help from other people and social services, suggesting that their IADL abilities were relatively high. In fact, a previous epidemiological study showed that people with depressive status had significantly lower scores of IADL compared to those without depressive status, which was clearer in people aged 65 to 74 years (p = 0.01) than in people aged 75 years and older (p = 0.07) [7]. However, this particular study did not aim to detect differences between the age groups on the association, and it did not conduct a statistical test for the possible age-group differences. On the contrary, the present study directly compared the possible difference between age groups, specifically 70s and 80s, on the association of depressive symptoms with IADL decline within 3 years by multiple group analysis which a significant difference. Additionally, the present study used a longitudinal design, though the previous study used a cross-sectional design.
In the present study, we could suggest the association between depressive symptoms and IADL decline may change by the age groups, 70s and 80s. Health professionals should take care of IADL decline when their patients in their 70s have depressive symptoms. On the other hand, health professionals should pay attention to other potential risks (e.g., cognitive decline) rather than IADL decline even when their patients in their 80s have depressive symptoms.
Strengths and limitations
We had the following strengths. We directly investigated differences between the two age groups on the association of depressive symptoms with IADL decline because previous studied did not investigate the possible differences even though prevalence of depression symptoms and IADL decline were different between the age groups. The present study used a longitudinal design, which allowed us to decide temporal order on the association of depressive symptoms with IADL decline.
Nevertheless, the present study had the following limitation. First, in the present study, IADL and depressive symptoms were assessed by a self-reported questionnaire. IADL was assessed by TMIG index of competence. However, reliability coefficients indicated high reliability of the TMIG Index of Competence (the reliability coefficient Alpha was 0.91; the 1-year test-retest reliability coefficient was 0.86) [2].
Additionally, depressive symptoms were assessed by GDS-5 that was a self-reported questionnaire. However, GDS-5 had a sensitivity of 0.97 and a specificity of 0.85 for depressive symptoms assessed by Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition (DSM-IV) criteria [10]. Second, there could be residual confounding factors such as marital status and occupation. However, the present study considered the following possible confounders: sex, age, cognitive function, body mass index, histories of stroke and heart diseases, economic condition, education, hypertension, dyslipidemia, and diabetes mellitus.
Conclusion
The present study showed that the association of depressive symptoms with IADL decline within 3 years was different between the age groups of 70s and 80s. Interestingly, the 70s age group had a significant association, while the 80s did not. Prevention of IADL decline should be planned considering the age group; for example, detecting depressive symptoms may be a key for preventing IADL decline in elderly people in their 70s and not for those in their 80s. Health professionals should pay attention to other risks related to aging rather than IADL decline when their patients in their 80s have depressive symptoms.
Availability of data and materials
The datasets used and/or analyzed during the current study available from the corresponding author on reasonable request.
Abbreviations
- AIC:
-
Akaike information criterion
- CI:
-
Confidence interval
- IADL:
-
Instrumental activities of daily living
- MoCA-J:
-
Japanese version of the Montreal Cognitive Assessment
- OR:
-
Odds ratio
- RMSEA:
-
Root mean square error of approximation
References
for Community Living A. A Profile of Older Americans: 2017. https://acl.gov/sites/default/files/AgingandDisabilityinAmerica/2017OlderAmericansProfile.pdf. Accessed 5 May 2019.
Koyano W, Shibata H, Nakazato K, Haga H, Suyama Y. Measurement of competence: reliability and validity of the TMIG index of competence. Arch Gerontol Geriatr. 1991;13(2):103–16.
Kondo N, Kazama M, Suzuki K, Yamagata Z. Impact of mental health on daily living activities of Japanese elderly. Prev Med (Baltim). 2008;46(5):457–62.
Hybels CF, Pieper CF, Blazer DG. The complex relationship between depressive symptoms and functional limitations in community-dwelling older adults: the impact of subthreshold depression. Psychol Med. 2009;39(10):1677–88.
Liang Y, Welmer A-K, Möller J, Qiu C. Trends in disability of instrumental activities of daily living among older Chinese adults, 1997-2006: population based study. BMJ Open. 2017;7(8):e016996.
Interagency Forum on Aging-Related Statistics F. Older Americans 2016: Key Indicators of Well-Being. http://www.dol.gov/ebsa. Accessed 24 Apr 2019.
Ormel J, Kempen GI, Deeg DJ, Brilman EI, van Sonderen E, Relyveld J. Functioning, well-being, and health perception in late middle-aged and older people: comparing the effects of depressive symptoms and chronic medical conditions. J Am Geriatr Soc. 1998;46(1):39–48.
Ishizaki T, Kai I, Kobayashi Y, Imanaka Y. Functional transitions and active life expectancy for older Japanese living in a community. Arch Gerontol Geriatr. 2002;35(2):107–20.
Rinaldi P, Mecocci P, Benedetti C, Ercolani S, Bregnocchi M, Menculini G, et al. Validation of the five-item geriatric depression scale in elderly subjects in three different settings. J Am Geriatr Soc. 2003;51(5):694–8.
Hoyl MT, Alessi CA, Harker JO, Josephson KR, Pietruszka FM, Koelfgen M, et al. Development and testing of a five-item version of the geriatric depression scale. J Am Geriatr Soc. 1999;47(7):873–8.
Ogata S, Hayashi C, Sugiura K, Hayakawa K. Associations between depressive state and impaired higher-level functional capacity in the elderly with long-term care requirements. PLoS One. 2015;10(6):e0127410 Laks J, editor.
Yamazaki S, Nakano K, Saito E, Yasumura S. Prediction of functional disability by depressive state among community-dwelling elderly in Japan: a prospective cohort study. Geriatr Gerontol Int. 2012;12(4):680–7.
Fujiwara Y, Suzuki H, Yasunaga M, Sugiyama M, Ijuin M, Sakuma N, et al. Brief screening tool for mild cognitive impairment in older Japanese: validation of the Japanese version of the Montreal cognitive assessment. Geriatr Gerontol Int. 2010;10(3):225–32.
Nasreddine ZS, Phillips NA. Bédirian V, Charbonneau S, whitehead V, Collin I, et al. the Montreal cognitive assessment, MoCA: a brief screening tool for mild cognitive impairment. J Am Geriatr Soc. 2005;53(4):695–9.
Kario K. Key points of the Japanese society of hypertension guidelines for the management of hypertension in 2014. Pulse (Basel, Switzerland). 2015;3(1):35–47.
Teramoto T, Sasaki J, Ishibashi S, Birou S, Daida H, Dohi S, et al. Diagnosis of atherosclerosis. Executive summary of the Japan atherosclerosis society (JAS) guidelines for the diagnosis and prevention of atherosclerotic cardiovascular diseases in Japan—2012 version. J Atheroscler Thromb. 2014;21(4):296–8.
Haneda M, Noda M, Origasa H, Noto H, Yabe D, Fujita Y, et al. Japanese clinical practice guideline for diabetes 2016. J Diabetes Investig. 2018;9(3):657–97.
Muthén BO. Latent variable modeling in heterogeneous populations. Psychometrika. 1989;54(4):557–85.
Deng L, Yuan K-H. Multiple-group analysis for structural equation modeling with dependent samples. Struct Equ Model Multidiscip J. 2015;22(4):552–67.
Muthén L, Muthén BM-M and, 2010. 1998–2010 Mplus user’s guide. Los Angeles . https://scholar.google.com/scholar_lookup?title=Mplus+User’s+Guide&author=LK+Muthén&author=BO+Muthén&publication_year=1998–2012&. Accessed 29 May 2019.
Gurland BJ, Wilder DE, Berkman C. Depression and disability in the elderly: reciprocal relations and changes with age. Int J Geriatr Psychiatry. 1988;3(3):163–79.
Stek ML, Vinkers DJ, Gussekloo J, Van Der Mast RC, Beekman ATF, Westendorp RGJ. Natural history of depression in the oldest old. Br J Psychiatry. 2006;188(1):65–9.
Kiyoshige E, Kabayama M, Sugimoto K, Arai Y, Ishizaki T, Gondo Y, et al. Difference in association of depression with IADL decline between 70s and 80s age groups. Innov Aging. 2018;2(Suppl 1):943.
Acknowledgements
We gratefully thank all staff involved in the SONIC study, especially Prof. Shin-ichi Satoh, Ms. Yoshiko Ishioka, Ms. Megumi Tabuchi, Ms. Yukiko Tatsuhira, and Ms. Marina Kozono at Osaka University, Graduate School of Human Sciences, Dr. Koichi Yamamoto, Dr. Yasushi Takeya, Dr. Yoichi Takami, Dr. Ryousuke Oguro, Dr. Serina Yokoyama, Dr. Satomi Maeda, Dr. Masanori Nagasawa, Dr. Taku Fujimoto, Dr. Hirochika Ryuno, Ms. Kayo Godai, Mr. Yuya Akagi at Osaka University Graduate School of Medicine, Prof. Yoshinobu Maeda, Prof. Shin-ya Murakami, Dr. Masahiro Kitamura, Dr. Ryosuke Kagawa, Dr. Ken-ichi Matsuda, Dr. Tadashi Okada, Dr. Chisato Inomata, Dr. Hajime Takeshita, Dr. Yusuke Mihara, and Dr. Masahiro Uota at Osaka University Graduate School of Dentistry, and Takeshi Kurinobu at Tokyo Metropolitan Geriatric Hospital and Institute of Gerontology. They were responsible in collecting data in the SONIC study. We also thank Ms. Yumiko Aoshima and Ms. Tae Matsue, at Osaka University, Graduate School of Medicine for secretarial work. We sincerely appreciate all SONIC participants for their kind cooperation. Additionally, the present study is an extended version of a study presented at the Gerontological Society of America 2018 annual scientific meeting [23].
Funding
This study was supported in part by grants-in-aid from the Ministry of Education, Culture, Sports, Science and Technology of Japan (KK: 2510211, 15 K08910, MK: 16 K12336), and the Pfizer Health Care Research Foundation (to KK). Additionally, this work was supported by JSPS KAKENHI Grant Number JP19J12740. The funders had no role in the study design, data collection and analysis of the data.
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EK is the first author. Additionally, EK conducted the statistical analysis, interpreted the data, and wrote the manuscript; YG, YM, KI, YA, TI, HR, and KK were responsible for designing the SONIC Study and for data collection; EK, MK, HA, KS, YA, TI, HR, and KK were responsible for collecting medical and biological data; YG, YM, HI, MO, TN, and SY were responsible for collecting psychological and sociological data. All authors developed the survey and read and approved the final manuscript.
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This study was conducted according to the guidelines laid down in the Declaration of Helsinki and approved by the Institutional Review Board of Osaka University Graduate School of Medicine, Dentistry and Human Sciences and the Tokyo Metropolitan Institute of Gerontology (approval numbers 266, H22-E9, 22,018, and 38, respectively). Written informed consent was obtained from all participants.
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Additional file 1: Table S1.
Adjusted Odds Ratios (95%CI) of Depressive symptoms for each baseline characteristic stratified by age groups (70s and 80s) and depressive status.
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Kiyoshige, E., Kabayama, M., Gondo, Y. et al. Age group differences in association between IADL decline and depressive symptoms in community-dwelling elderly. BMC Geriatr 19, 309 (2019). https://doi.org/10.1186/s12877-019-1333-6
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DOI: https://doi.org/10.1186/s12877-019-1333-6